BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HANDTYMP SCREENER MODEL 2000 + 2002 REMOTE TRANS.

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    EPIC II PLUS DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·November 10, 2010

    MARYLAND BIPOLAR FORCEPS

    FDA Adverse Event
    INTUITIVE SURGICAL,INC.·Product code NAY·January 3, 2013

    OT VERIO PRO PLUS METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 26, 2014